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1956 L. G. S. BROOKER ET AL 2,

SENSITIZED PHOTOGRAPHIC SILVER HALIDE EMULSIONS Original Filed Out. 4, 1952 Jill HMFITM nu mun 1m 9 (p-ACETOPHENETIDIDO)-3,3" DIMEI'HYLTHIACARBOCYANINE p- TOLUENESULFONATE ml IILI/ IIITNHH 9"ACETAN|LlD0"3,3" DIMETHYLTHIACARBOCYANINE P TOLUENESULFONATE Fig.5

klm Ill/WWW llll IILLWTFN m 9" (P-ACETOPHENETIDIDO) 3,3" DIMETHYL'4,5,4:5"DIBENZO- THIACARBOCANINE CHLORIDE leslieGSlBmoker Frank L.Whiie INVENTORS ATTORNEYS United States Patent SENSITIZED PHOTOGRAPHIC SILVER HALIDE. EMULSIONS Leslie S. Brooker and Frank L. White, Rochester, N. Y., assignors to Eastman Kodak Company, Rochester, N. Y., a corporation of New Jersey Original application October. 4, 1952, Serial No. 313,194,

now abandoned. 16, 1954, SeriaLNo. 437,110

9,.Claims; (Cl. 95 7) This invention relates to photographic emulsions containing new carbocyanine dyes.

The new carbocyanine dyes used in our invention can he represented by the following general formula:

wherein R and R each represents an alkyl group,.such as methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, benzyl (phenylmethyl), fi-phenylethyl, ,B-hydroxyethyl, carbomethoxymethyl, fl-carbomethoxyethyl, etc., R2 represents an acyl group, such as acetyl, propionyl, n-butyryl, isobutyryl, benzoyl, 0.-, m-, and p-toluyl, o-, m-, and pmethoxybenzoyl, etc., R3 represents a hydrogen atom, an alkyl group, such-.as-methyl, ethyl,.n-propyl, isopropyl, n-amyl, nrheptyl, n-octyl, etc., or an aromatic group, such asiphenyl, o-, m-, and'p-tolyl, a-naphthyl, ,B-naphthyl, 0-, m-, and'p-chl'orophenyl, o-, m-, and p methoxyphenyl, o-, the, and 'p-ethoxyphenyl, etc., X represents an acid radical, suchas chloride, bromide, iodide, perchlorate, thiocyanate, benzenesulfonate, p-toluenesulfonate, methylsulfateacthylsulfate,.etc., and Z and Z1 each represents the non-metallicatoms necessary to complete aheterocyclic nucleus.selected'from those of the benzothiazoleseries, such as benzothiazole, 5.-rnethylbenzothiazole, S-ethylbenzothia-zole, 5-chlorobenzothiazole, 5 bromobenzothiazole,= fi-methylbenzothiazole, 6-ethylbenzothiazole, 6- clilorobenzothiazole, 6-bromobenzothiazole, 5-methoxybenzotlriazole;v 5-.ethoxybenzothiazole, 6-rnethoxybenzothiazole, 6-ethoxybenzothiazole, 5-phenylbenzothiazole, 6' phenylbenzothiazole, S aminobenzothiazole, 6-aminobenzothiazole; 5-dimethylaminobenzothiazole, etc., and those of the naphthothiazole series, suchas u-naphthothiazole; .lirnaphthothiazole, etc.

It is, therefore; anobject of our invention to provide new carbocyanine dyes. Still another object is to provide a method for makingthese new dyes. Another object is to provide photographic silver halide emulsions sensitized with these new dyes. Other objects will become apparent from a consideration of the following description and examples.

In accordance with our inventionthe dyes of Formula I above wherein R2 represents an acyl group can be prepared by acylation of the corresponding dyes of Formula I above wherein R2 represents a hydrogen atom. Useful; acylating agents comprise organic carboxylic anhydrides, such as acetic anhydride, propionic anhydride, n-butyric, anhydride, isobutyric anhydride, benzoic anhydride, etc. The acylations are advantageously: efiected inthe; presence, of an inert solvent, such as pyridine; quinoline, .acetic acid, etc.

According to our invention we provide the dyes" of Formula I" above whereinRzrepresentsa hydrogen atom Divided and this application June 7 2,735,770 Eatented Feb. 21, 1956 by reacting together a dye selected from those represented by the following general formula:

wherein R, R1, X, Z and Z1 each have the values given above, and R4 represents an alkyl group, such as methyl, ethyl, etc., or an aromatic group, such as phenyl, o-, m-, and p-tolyl, etc.,'with ammonia or a primary amine selected from those represented bythefollowing general formula: PI R3NH2 where R3 has the values given above. Heat: accelerates the reaction and inert solvents, such as pyridine, quinoline, etc. can be used if desired. The dyes of Formula II above can be prepared in accordance with the method described in Brooker and White U. S. Patent 2,520,358 issued August 29, 1950.

The following examples will serve-to illustrate more fully the manner whereby we prepare these dyes.

Example 1.-9-anilina-3,3'-dimethylthiacarbocyaniile p-toluenesulfonate A mixture of 2.77 grams (1 mol.) of 3,3.'-dimethyl-9- methylmercaptothiacarbocyanine p-toluenesulfonate, 5.12 grams (1 mol.|1000% excess) of aniline and 20 m1. of dry pyridine was heated at the refluxing temperature-for 15 minutes. The cool, much lighter-colored reaction mixture was stirred with 250 ml. of ether. After chilling, the solid was collected on a filter and washed with ether. The residue was stirred, in a beaker, with hot acetone. After chilling, the dye was collected on a filter. and washed with acetone. The yield of dye was percent crude and 50 percent after two recrystallizations from ethyl alcohol. The dull orange-red crystals had melting point 186-187 C. with decomposition and they sensitized a photographic gelatino-silver-bromoiodide emulsion.

to about 650 mu with maximum sensitivity at about 600 mu.

By replacing the aniline used in the above example by a molecularly equivalent amount of p-cyanoaniline, 9- (p cyanoanilino) 3 3' dimethylthiacarbocyanine p toluenesulfonate was obtained as deep-colored crystals.

The dyes of Examples 2 to 7 below were prepared in a manner similar to that described in Example 1 above, except that another organic primary amine was substituted for the aniline of that example.

Example 2 .9- m-ch loroanilirto -3,3 '-dimethylth iacqrbocyanine p-toluenesulfonate 9- (rn-chloroanilino) -3, 3 '-dimethylthiacarbo'cyanine ptoluenesulfonate was prepared by using 6.38 grams of m-chloroaniline in place of aniline'and heating the reac- 2,735,770 V t p tion mixture for 67 minutes at the refluxing temperature.

The red crystals with a green reflex had melting point 234235 C. with decomposition, and they sensitized a photographic gelatino-silver-bromoiodide emulsion to about 635 mu with maximum sensitivity at about 600 mu.

Example 3.3,3-dimethyl-9-p-phenetidinothiacarbocyanine p-toluenesulfonate 3,3'-dimethyl-9-p-phenetidinothiacarbocyanine p-toluenesulfonate was prepared by using 7.53 grams (1 mol.+1000% excess) of p-phenetidine in place of aniline. The orange crystals had melting point 229-230 C. with decomposition and they sensitized a photographic gelatino-silver-bromoiodide emulsion to about 625 mu with maximum sensitivity at about 595 mu.

Example 4.-3,3-dimethyl-9-p-t0luidin0thiacarbocyanine p-toluenesulfonate Example 5 .-3,3-dimethyl-9-m-loluidinotlziacarbocyanine p-toluenesulfonate S 3,3'-dimethyl-9-m-toluidinothiacarbocyanine p-toluenesulfonate was prepared by using m-toluidine in place of aniline and heating the reaction mixture at the refluxing temperature for 50 minutes. The amber needles with green reflex had melting point 147-149 C. with decomposition and they sensitized a photographic gelatinosilver-bromoiodide emulsion to about 640 mu with maximum sensitivity at about 600 mu.

CHI

Example 6.9-n-heptylamin0-3,3'-dimethylthiacarbocyanine p-toluenesulfonate 9-n-heptylamino-3,3'-dimethylthiacarbocya.nine p-toluene-sulfonate was prepared by using 3.45 grams (1 mol.+500% excess) of n-heptylamine in place of aniline. The orange crystals, from ethyl alcohol plus ether, had melting point l44146 C. with previous softening, and they sensitized a photographic gelatino-silver-chlorobromide emulsion to about 530 mu with maximum sensitivity at about 500 mu.

Example 7.9-benzylamino-3,3-dimethylthiacarbocyanine p-toluenesulfonate S S \C=CH-C=CHC/ NH N Example 8.9-amin0-3,3'-dimethylthiacarbacyanine p-toluene-sulonate 9-amino-3,3-dimethylthiacarbocyanine p-toluenesulfonate was prepared by passing dry ammonia gas into a suspension of 27.5 grams of 3,3'-dimethyl-9-methylmercaptothiacarbocyanine p-toluenesulfonate in 200 ml. of dry pyridine containing 7.3 grams of triethylamine. As the ammonia was added, the reaction mixture was kept at about C. for one hour, the addition of the ammonia was discontinued, the reaction mixture was allowed to stand overnight and the next day ammonia was added slowly as the reaction mixture was heated at about 115 C. for minutes. The cool reaction mixture was stirred with ether. After chilling, the dye was collected on a filter and washed with ether. The yield was 24.0 grams. The methyl alcoholic solution of the brownish-orange crystals was yellow.

Example 9.-3-ethyl-3'-methyl-9-p-phenetidinothiacarbocyanine p-loluenesulfonate A mixture of 2.84 grams (1 mol.) of 3-ethyl-3'-methyl- 9 methylmercaptothiacarbocyanine p toluenesulfonate, 4.11 grams (1 mo1.+500% excess) of p-phenetidine and 10 ml. of dry pyridine was heated at the refluxing temperature for 30 minutes. The cool reaction mixture was stirred with 250 ml. of ether. After chilling, the solid was collected on a filter and washed with ether. The residue was stirred, in a beaker, with 25 ml. of hot acetone.

Example 10.3,3'-dimethyl-9-p-phenetidin0-4,5;4,5'- dibenzpthiq r ocyanin hl id A mixture of 0.87 gram (1.mol.) of r3, 3'-dimet hyl-9- methylmercapto-. 4,5;4,-5frdibenzothiacarbocyanine .chloride, 2.5 l gr ams (1 mol.+1000% excess) of p-phenetidine and 10 m1. of dry pyri dine washeated at therefiuxing temperatpreior 7 minutes. The cool reaction mixture was stirred with ether. After chilling, the solid was collected on a filter and washed with ether. The residue was stirred, in a beaker, with hot acetone. After chilling, the

dye was collected ona filter and washed with acetone. The yield of dyeflw as 97' percent crude and 49 percent after two recrystallizations from ethyl alcohol. The yery dark green crystals had melting point 210- 211 with decomposition and they sensitized a photographicgelatinosilver-bromoiodide emulsion to about 680 mu with maximum sensitivity about 650 mu.

Example 1l.- 9-(p-acetophenetidido)-3,3'-dimetlrylthiacarb'oeyanine p-toluenesulfonate .Amixture, of 1.29 grams l mol.) ,of -3,3f.-dimelhYl-9 p-phenetidinothiacarbocyanine ,p-toluenesulfonate, 1. 22 grams .(;1 -rnol.,-|-.500% excess) of acetic anhydrideand .1-5 rml. of. pyridine washeated at therefluxing temperature for 7 minutes. ,The cool reaction mixture was stirred .withQfiOnrrL of ether. After chilling overnight,,the, solid .was collected on .a filter-and washed with ether. The residue was stirred, in a beaker, with hotacetone. -;'l ;he .suspensionwas chilled, ;the .dye wascollectedon a filter and yvashedwith acetone. The yield of dye was l9 per- ,cent crude and 5 8.percentafter two recrystallizationsirom nitromethane. The darkgreencrystals had melting; pgint 19l -192 C. with decomposition andthey i sensitiaed a photographic gelatino silver-bromoiodide emulsion to about 645 rnu with maximum sensitivity at about 625 mu.

Example 12.9 (m-chloroacetanilido -3,3'-dir ne thylthiacarbocyanine p-toluenesulfonate when :(m-h .anilin ):3. 'rrlimethy y nine p-toluenesulfonate was acetylated, 9-(m-chloroacetanilido) -3,3'-dimethylthiacarbocyanine p-toluenesulfonate was isolated as,dark crystals with a green reflux from ethyl alcohol. The dye had melting point 2 06-2Q9 C. with decomposition and it sensitizeda photographic gelatino-silyer bromoiodide emulsion to about 640 mu with maximum sensitivity .at about 625 mu.

Example 13.9-acetanilid0-3,3Gdimethylthiacarbocy anin e p-tolue ne sulfo n ate When 9-anilino-3,3'-dimethylthiacarbocyanine p-toluenesulfonate was acetylated, 9-acetanilido-3,3'-dimethylthiacarbocyanine p-toluenesulfonate was isolated as. dark bluish crystals from nitromethane.plus;a.little ether. The dye had meltingpoint 188 189 (I. with decomposition and it sensitized a photographic gelatino-silvenbromoiodide er'nulsionto about .650 mu with maximum sensitivity at abql t 625 mu.

The acetylations in Examples l2 and 13 above were carried out in the same manner as the acetylation described in Example 11.

eEgcample-14.9 (p-acet ophentzjdido) -3-e thyl;'3'-methylthiaeai-bocyarpine p-tpluensulforiate INTCQCHQ\ A mixture of 2.84 grams (1 mol.) of .3-ethyl- 3'-methyl- 9 methylmercaptothiacarbocyanine p-toluenesulfonate, 7.54 grams r1 mol.+1000% excess) of p-phenetidine and 10 ml.. of.drypyridine-were-heated together'atthe refluxing ternperaturefor 20 minutes. The cool reaction mixture was stirred with 250 ml. of ether. After chilling, the solid was/collected on a filter and washed with ether. The residue was stirred, in a beaker, with 35 ml. of hot acetone. After chilling the suspension, the dye was collected on a filter and washed with acetone.

:1 1 rad -n-nh nefidi e ye 1 am wa hea w t @19 ram 1 9l-+ :5Q0% e ess) .Q a s aaqhyari I 0m of Pyridin a he r fl i e smp amm o 7 .m nut s- The 0 rea tion tu was stirre a,with-200-,rnl.,-of ether. After chilling, the solid .wascol- :lected .on :the filter and washed with ether. vwasstirred, inabeaker, with hot acetone. Thesuspen- The residue lfizsd .a hqto r rhl ce t P Yu-bIQmQiQd sk emulsi n to about 630 mu with sensitivity a aha!! 620 mu.

7 Example I5.-9-m-acetotoluidido-3,3-dimethylthiacarbocyanine p-toluenesulfonate I l- C H:\

N HI on: OsmQ-mm 9-m-acetotoluidido 3,3 dimethylthiacarbocyanine ptoluenesulfonate was obtained by acetylating the corresponding crude 9-m-toluidin0 dye, which was prepared from m-toluidine and 3,3'-dimethyl-9-methylmercaptothiacarbocyanine p-toluenesulfonate. The bluish crystalline powder of the acetylated dye decomposed from about 152 C. and it sensitized a photographic gelatino-silverbromoiodide emulsion to about 640 mu with maximum sensitivity at about 625 mu.

Example I6.9-p-acetotoluidido-3,3-dimethylthiacarbocyanine p-toluenesulfonate Example 1 7.9- (p-acetophenetidido) -3,3 '-dimethyl- 4,5;4,5-dibenz0thiacarbocyanine chloride OCIH] A mixture of 0.35 gram (1 mol.) of 3,3-dimethyl-9-pphenetidino-4,5;4',5'-dibenzothiacarhocyanine chloride, 0.56 gram (1 mol.+1000% excess) of acetic anhydride and 5 ml. of dry pyridine was heated at the refluxing temperature for 7 minutes. The cool reaction mixture was stirred with ether. After chilling, the solid was collected on a filter and washed with ether. The residue was stirred, in a beaker, with hot acetone. After chilling, the dye was collected on a filter and washed with acetone. The yield of dye was 0.23 gram crude and 0.08 gram after two recrystallizations from ethyl alcohol. The purplish crystalline powder had melting point l87-189 C. with decomposition and it sensitized a photographic gelatino-silverbromoiodide emulsion to about 685 mu with maxlmum sensitivity at about 670 mu.

8 Example 18.-9-N-n-heptylacetamido-3,3'-dz'methylthiacarbocyanine p-toluenesulfonate N/ E;COCHI\N When 9-n-heptylamino-3,3'-dimethy1thiacarbocyanine p-toluenesulfonate was acetylated, 9-N-n-heptylacetamido- 3,3'-dimethylthiacarbocyanine p-toluenesulfonate was isolated as pale bluish-green crystals, melting at 220-221 C. with decomposition, and they sensitized a photographic gelatino-silver-bromoiodide emulsion to about 645 mu with maximum sensitivity at about 630 mu.

Example I9.9-N-benzylacetamid0-3,3'-dimethylthiacarbocyanine p-toluenesulfonate When 9-benzylamino-3,3-dimethylthiacarbocyanine ptoluenesulfonate was acetylated, 9-N-benzylacetamido- 3,3'-dimethylthiacarbocyanine p-toluenesulfonate was isolated as dark red crystals with a green reflux melting at 223-224 C. with decomposition, and they sensitized a photographic gelatino-silver-bromoiodide emulsion to about 640 mu.

20. 3,3'-dimethyl-9-N-,B-naphthylacetamidothiacarbocyanine p-toluenesulfonate Example 21.9-acetamido-3,3-dimethylthiacarbocyanine p-toluenesulfonate When 9-arnino-3,3'-dimethylthiacarbocyanine p-toluenesulfonate' was acetylated, 9-acetamido-3,3'-dimethylthiacarbocyanine p-toluenesulfonate was isolated as cop- Example pery crystals, meltingat- 208-210 C. with decomposition, and they sensitized a photographic gelatino-silver-chlorobromide emulsion to, about595 muflwith maximum sensitivity at about 560, mu.

The acetyl ations ofExampleslS, to 21 were carried out ,inthe same manneras that of Example 17. In a similar manner, the dyes of Formula I wherein R2 is hydrogen can hbeacylatedwith othercarboxylic anhydrides, such as pro- ..pionic ,anhydride, .n-butyric anhydride, isobutyric anhydride, benzoic anhydride, etc.

As shown above we have found that our new dyes spectrally sensitize photographic-silver halideemulsionswhen incorporated therein. The dyes are especially useful for extending the spectral sensitivity of the customarily employed gelatino;si lver-chloride, .gelatino-silver-chlorobromide, gelatino-silver-bromide and gelatino-silverbromiodide' developing-out emulsions. To prepare emulsions sensitized with one or more of our new dyes, it is ,o nly pcgess ary to disperse the dye or. dyes in the emulsions.

methods of i nco rporatingi dyes in: emulsions are, simple and are known to those skilled in the art. In practice, it is convenient to add the dyes to the emulsions in the form of a solution in an appropriate solvent. Methanol or acetone has proved satisfactoryas a solvent for most of our new dyes. Where the. dyes .are quite insoluble in methylalcohol, a mixture of methyl. alcohol and pyridine is advantageously employed as a solvent. The dyes are advantageously incorporated in the finished, washed emulsions and should be uniformly distributed throughout the emulsions. The particular solvent used will, of course, depend on the solubility properties of the particular dye.

The concentration oftheldyes in the .emulsions can vary widely, e. g ft-om 5 to, 1 mg, per liter of flowableemulsion. The conc entration ofthe dyes will vary according t o 'the type of emulsion and accordingto the effect desir d. The suitable and most economical concentration for any given emulsion will be' apparent to those skilled in the art, upon making the ordinary tests and observations customarily used in the art of emulsion making. To prepare a gelatino-silver-halide emulsion sensitized with one or more of our new dyes, the following procedure is satisfactory.

A quantity of dye is dissolved in methyl alcohol or acetone (or a mixture of methyl alcohol and pyridine) and a volume of this solution, which may be diluted with Water, containing from to 100 mg. of dye, is slowly added to about 1000 cc. of gelatino-silver-halide emulsion, with stirring. Stirring is continued until the dye is thoroughly dispersed in the emulsion.

With most of our dyes, from to mg. of dye per liter of gelatino-silver-bromide or bromoiodide emulsion (containing about 40 g. of silver halide) suffices to produce the maximum sensitizing effect. With the finer grain emulsions, somewhat larger concentration of dye may be needed to produce the maximum sensitizing effect.

The above statements are only illustrative, as it will be apparent that the dyes can be incorporated in photographic emulsions by any of the other methods customarily employed in the art, e. g. by bathing a plate or film upon which an emulsion is coated in a solution of the dye in an appropriate solvent. However, bathing methods are ordinarily not to be preferred. Emulsions sensitized with the dyes can be coated on suitable'supports, such as glass, cellulose derivative film, resin film or paper in the usual manner.

The accompanying drawing further illustrates our invention. Each figure is a diagrammatic reproduction of a spectrogram showing the sensitivity of an ordinary gelatino-silver-bromiodide Y emulsion containing one of our sensitizing dyes. In Fig. 1, the curve depicts the sensitivity of an ordinary gelatino-silver-bromiodide emulsion containing 9-(p-acetophenetidido)-3,3'-dimethylthiacarbocyanine p-toluenesulfonate. In Fig. 2, the curve depicts the sensitivity of an ordinary gelatino-silverbromiodide emulsion containing 9-acetanilido-3,3-dimethylthiacarbocyanine p -toluen esulfonate. In 3,

the curve depicts thesensitivity of anordinary gelat inosilver-bromiodide emulsion containing 9-(p-ac letophenwherein R and R1 each represents an alkyl group, Ra represents a member selected from the group consisting of a hydrogen atom, an alkyl group, and an aromatic carbocyclic group, X represents an acid radical, and Z represents the non-metallic atoms necessary to complete a heterocyclic nucleus selected from the group consisting of those of the benzothiazole series and those of the naphthothiazole series.

i 2. A photographic silver halide emulsion sensitized with a symmetrical carbocyanine dye selected from those represented by the following general formula:

wherein R and R1 each represents an alkyl group containing from 1 to 4 carbon atoms, R3 represents a member selected from the group consisting of a hydrogen atom, an alkyl group containing from 1 to 8 carbon atoms, and an aromatic carbocyclic group containing in addition to the carbon atoms only atoms selected from t the group consisting of chlorine, bromine, hydrogen, and oxygen, and Z represents the non-metallic atoms necessary to complete a heterocyclic nucleus selected from the group consisting of those of the benzothiazole series and those of the naphthothiazole series.

3. A photographic silver halide emulsion sensitized with a symmetrical carbocyanine dye selected from those represented by the following general formula:

wherein R and R1 each represents an alkyl group containing from 1 to 4 carbon atoms, R3 represents an aromatic carbocyclic group containing in addition to the carbon atoms, only atoms selected from the group consisting of chlorine, bromine, hydrogen, and oxygen, and Z represents the non-metallic atoms necessary to complete a heterocyclic nucleus of the benzothiazole series. 4. A photographic silver halide emulsion sensitized with a symmetrical carbocyanine dye selected from those represented by the following general formula:

wherein R and R1 each represents an alkyl group containing from 1 to 4 carbon atoms, R3 represents an aromatic carbocyclic group containing in addition to the carbon atoms, only atoms selected from the group con- 8 sisting of chlorine, bromine, hydrogen, and oxygen, X

represents an acid radical, and Z represents the non- I metallic atoms necessary to complete a heterocyclic I nucleus of the naphthothiazole series. 5 N COCH\N/ 5. A photographic silver halide emulsion sensitized on (5H, on oso on with the carbocyanine dye having the following formula: 3 7 3 8. A photographic silver halide emulsion sensitized with the carbocyanine dye having the following formula:

I OOsHs 20 9. A photographic silver halide emulsion sensitized with the carbocyanine dye having the following formula:

6. A photographic silver halide emulsion sensitized with the carbocyanine dye having the following formula:

N (11H: Cfia \CI l References Cited in the file of this patent 2 5 UNITED STATES PATENTS 7. A photographic silver halide emulsion sensitized 35 2,066,966 Dieterle et a1. Jan. 5, 1937 with the carbocyanine dye having the following formula: 2,066,968 Dieterle et a1. Jan. 5, 1937 2,637,729 Kendall et al. May 5, 1953 

1. A PHOTOGRAPHIC SILVER HALIDE EMULSION SENSITIZED WITH A SYMMETRICAL CARBOCYANINE DYE SELECTED FROM THOSE REPRESENTED BY THE FOLLOWING GENERAL FORMULA: 